Erik de Vrieze
8PUBLICATIONS
53CO-AUTHORS
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Publications (8)
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|Apr 10, 2026
FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.Daniel Liedtke, Kristen Rak, Katrina M Schrode
|Mar 04, 2025
Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches.Merel Stemerdink, Tabea Riepe, Nick Zomer
|Jul 17, 2023
Succinic semialdehyde dehydrogenase deficiency in mice and in humans: An untargeted metabolomics perspective.Tessa M A Peters, Udo F H Engelke, Siebolt de Boer
|Jun 28, 2023
Generation and Characterization of a Zebrafish Model for ADGRV1-Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing Technology.Merel Stemerdink, Sanne Broekman, Theo Peters
|Feb 25, 2022
Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis.Sybren M M Robijn, Jeroen J Smits, Kadriye Sezer
|Sep 10, 2021
Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein Complexes.Erik de Vrieze, Suzanne E de Bruijn, Janine Reurink
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Frequent Collaborators
6 joint publications
Erwin van Wijk
5 joint publications
Hannie Kremer
2 joint publications
Suzanne E de Bruijn
2 joint publications
Merel Stemerdink
1 joint publications
Wim H Quint
1 joint publications
H Martijn de Gruiter
1 joint publications
Adam C Miller
1 joint publications
Caroline C W Klaver
1 joint publications
Adriana I Iglesias
1 joint publications
Renske Schellens
